A Study on the Effect of Food Containing Plant Extract on Vascular Endothelial Function. -A Ramdomized, Double-blind, Placebo-controlled, Parallel-group Study
- Conditions
- o
- Registration Number
- JPRN-UMIN000036602
- Lead Sponsor
- KSO Corporation
- Brief Summary
Statistically significant difference was confirmed in the primary outcome.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Not provided
(1) Subjects who contract chronic disease and are under treatment. (2) Subjects who can't stop using medicines, quasi-drugs, supplements and/or functional foods (including Food for Specified Health Uses or Foods with Function Claims) affecting blood pressure, lipid metabolism, blood sugar level, body fat, and so on during test periods. (3) Subjects who have a history of and/or contract serious diseases (eg, liver disease, kidney disease, digestive disease, heart disease, respiratory disease, endocrine disease, thyroid disease, adrenal disease and/or metabolic disease). (4) Subjects who have a history and/or a surgical history of digestive disease affecting digestion and absorption. (5) Subjects who are judged as unsuitable for the current study by screening tests. (6) Subjects who are diagnosed as arrhythmia by the screening tests. (7) Subjects who are shiftworker and/or midnight-shift worker. (8) Subjects who have declared allergic reaction to ingredients of test foods. (9) Subjects who have excessive alcohol intake more than approximately 60 g/day of pure alcohol equivalent or habit of drinking not less than 5 days a week. (10) Subjects who have a history of and/or contract drug addiction and/or alcoholism. (11) Subjects who can't stop drinking from 2 days before each measurement. (12) Subjects who have been pregnant or have a plan to become pregnant, or breast feed during the study period. (13) Subjects who have donated over 200 mL of blood and/or blood components within the last one month prior to the current study or over 400 mL of blood and/or blood components within the last three months prior to the current study. (14) Subjects who are planning to participate and/or had participated in other clinical studies within the last one month prior to the current study. (15) Subjects who are judged as unsuitable for the current study by the investigator for other reasons.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method FMD
- Secondary Outcome Measures
Name Time Method